A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690526



Internal ID15427178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128832927..128881377hg38UCSC Ensembl
Innerchr7:128472981..128521431hg19UCSC Ensembl
Innerchr7:128260217..128308667hg18UCSC Ensembl
Innerchr7:128066932..128115382hg17UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3848451
hg1948451
hg1848451
hg1748451
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517371
Supporting Variants
Samples
Known GenesATP6V1F, FLNC, KCP, LOC100130705
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690526
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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